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Diseases
Genes (270)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
GNAS
Fibrous Dysplasia Of Bone
Mccune-Albright Syndrome
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
DDX58
Singleton Merten Syndrome
ALB
Membranoproliferative Glomerulonephritis
Protein Losing Enteropathy
SOST
Craniodiaphyseal Dysplasia
CFB
Membranoproliferative Glomerulonephritis
PON1
Membranoproliferative Glomerulonephritis
DNASE2
Membranoproliferative Glomerulonephritis
C1QA
Membranoproliferative Glomerulonephritis
FH
Fumarase Deficiency
TGFBR2
Membranoproliferative Glomerulonephritis
Uterine Rupture